@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_head {
  this: np:hasAssertion dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_assertion;
    np:hasProvenance dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_provenance;
    np:hasPublicationInfo dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_assertion a np:Assertion .
  
  dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_provenance a np:Provenance .
  
  dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0236642 a ncit:C7057 .
  
  dgn-gda:DGNcb46dc493d497032c7136356f665bf5a sio:SIO_000628 miriam-gene:4137, lld:C0236642;
    a sio:SIO_001121 .
}

dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_provenance {
  dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_assertion dcterms:description
      "[They include the largely sporadic Alzheimer's disease (AD), progressive supranuclear palsy, corticobasal degeneration, Pick's disease and argyrophilic grain disease, as well as the inherited frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:15615642;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP473960.RAdWAxp7GCHBvFcTPYziyX-9A8-3-nPt0mbhbI_PZUYA8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:19+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}